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860345P

Avanti

14:0 PC-d54

1,2-dimyristoyl-d54-sn-glycero-3-phosphocholine, powder

Synonyme(s) :

DMPC-D54

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About This Item

Formule empirique (notation de Hill):
C36H18NO8PD54
Numéro CAS:
Poids moléculaire :
732.27
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 10 mg (860345P-10mg)
pkg of 1 × 100 mg (860345P-100mg)
pkg of 1 × 200 mg (860345P-200mg)
pkg of 1 × 25 mg (860345P-25mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 860345P

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)COC(C([2H])([2H])C([2H])([2H])C([2H])([2H

InChI

1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1/i1D3,2D3,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2,18D2,19D2,20D2,21D2,22D2,23D2,24D2,25D2,26D2,27D2,28D2,29D2

Clé InChI

CITHEXJVPOWHKC-RPLUSTTMSA-N

Description générale

Deuterated fatty acids experience exchange of the deuteriums on the alpha carbon to the carbonyl, i.e., C2 position, and will therefore be a mixture of compounds that are fully deuterated and partially deuterated at that position.
Phosphocholine is a metabolic intermediate of phosphatidylcholine synthesis. Phosphorylation of choline in the presence of ATP yield phosphocholine.

Application

14:0 PC-d54 is suitable to reconstitute [ILV-13CH3, U-15N, 2H] labeled EmrE in n-dodecyl-β-D-maltopyranoside (DDM) back-exchanged to 1H at the amide positions during nuclear magnetic resonance (NMR) sample preparation. It is also suitable for the preparation of phospholipid liposomes.

Conditionnement

5 mL Amber Glass Screw Cap Vial (860345P-100mg)
5 mL Amber Glass Screw Cap Vial (860345P-10mg)
5 mL Amber Glass Screw Cap Vial (860345P-200mg)
5 mL Amber Glass Screw Cap Vial (860345P-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Souvent commandé avec ce produit

Code de la classe de stockage

11 - Combustible Solids


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Phosphatidylcholine and the CDP-Choline Cycle
Fagone P, et al.
Biochimica et Biophysica Acta, 1831(5) (2013)
Protonation of a glutamate residue modulates the dynamics of the drug transporter EmrE
Gayen A, et al.
Nature chemical biology, 12(3), 141-141 (2016)
Fusion of Legionella pneumophila outer membrane vesicles with eukaryotic membrane systems is a mechanism to deliver pathogen factors to host cell membranes
Jager J, et al.
Cellular Microbiology, 17(5), 607-620 (2015)
Alessio Ausili et al.
Langmuir : the ACS journal of surfaces and colloids, 36(4), 1062-1073 (2020-01-14)
Vitamin K1 and vitamin K2 play very important biological roles as members of chains of electron transport as antioxidants in membranes and as cofactors for the posttranslational modification of proteins that participate in a number of physiological functions such as
Jess Li et al.
The Journal of biological chemistry, 295(9), 2664-2675 (2020-01-25)
Engineering and bioconjugation of proteins is a critically valuable tool that can facilitate a wide range of biophysical and structural studies. The ability to orthogonally tag or label a domain within a multidomain protein may be complicated by undesirable side

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

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